# FDA recall Z-2579-2018

> **GE Healthcare, LLC** · Class II · device recall initiated 2018-05-24.

## Product

Discovery MI Digital Ready

## Reason for recall

DIGITAL ReadyCT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible  Power Supply).

## Distribution

Nationwide distribution to AL, CA, CO, FL, IL, IN, MA, MD, MI, MS, NC, NJ, NY,OH, OK, SC, TN, TX, VA.

## Key facts

- **Recall number:** Z-2579-2018
- **Recalling firm:** GE Healthcare, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-24
- **Report date:** 2018-08-08
- **Termination date:** 2019-02-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2579-2018

## Citation

> AI Analytics. FDA recall Z-2579-2018. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-2579-2018. Source: US FDA. Licensed CC0.

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